Disease-gene associations mined from literature

Human genes for Sipple syndrome

Sipple syndrome [DOID:0050430]

Multiple endocrine neoplasia type 2 (also known as "Pheochromocytoma and amyloid producing medullary thyroid carcinoma", "PTC syndrome," and "Sipple syndrome") is a group of medical disorders associated with tumors of the endocrine system. The tumors may be benign or malignant (cancer). They generally occur in endocrine organs (e.g. thyroid, parathyroid, and adrenals), but may also occur in endocrine tissues of organs not classically thought of as endocrine.

Synonyms:  Sipple syndrome,  DOID:0050430,  Sipple disease,  Sipple disorder,  multiple endocrine neoplasia II ...

Linkouts:  OMIM